Restriction Enzymes PvuII

A restriction enzyme or restriction endonuclease is defined as a protein that recognizes a specific, short nucleotide sequence and cuts the DNA only at or near that site, known as restriction site or target sequence. The four most common types of restriction enzymes include: Type I (cleaves at sites remote from a recognition site), Type II (cleaves within or at short specific distances from a recognition site), Type III (cleave at sites a short distance from a recognition site), and Type IV (targets modified DNA- methylated, hydroxymethylated and glucosyl-hydroxymethylated DNA). The most common challenges with restriction digest include- 1. inactivation of the enzyme, 2. incomplete or no digestion, and 3. unexpected cleavage. The enzyme should always be stored at -20C and multiple freeze-thaw cycles should be avoided in order to maintain optimal activity. Always use a control DNA digestion with the enzyme to ensure adequate activity (to avoid interference due to high glycerol in the enzyme). For complete digestion, make sure that the enzyme volume is 1/10th of the total reaction volume, the optimal temperature is constantly maintained throughout the reaction, the total reaction time is appropriately calculated based on the amount of DNA to be digested, appropriate buffers should be used to ensure maximal enzymatic activity, and in case of a double digest, make sure that the two restriction sites are far enough so that the activity of one enzyme cannot interfere with the activity of the other. Star activity (or off-target cleavage) and incomplete cleavage are potential challenges which may occur due to suboptimal enzymatic conditions or inappropriate enzyme storage. To avoid these, follow the recommended guidelines for storage and reactions, and always check for the efficacy of digestion along with purification of digested products on an agarose gel.

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Found 4 matching solutions for this experiment

PvuII (10 U/µL)

Thermo Fisher Scientific

Protocol tips
The second dimension was run until the fragment of interest had migrated ∼10 cm. For long-range 2D AGEs, 5 μg of mitochondrial nucleic acids was digested with FastDigest BamHI or PvuII (Thermo Scientific), which cut mtDNA only once, and run on a 0.28% agarose gel in 1× TBE until the linearized mtDNA fragment had migrated 10 cm into the gel.
PvuII-HF®

New England BioLabs

Protocol tips
Digest a high copy number plasmid backbone (see materials) with PvuII-HF and PstI-HF at 37 °C for 1 hr (see Table 5) according to the manufacturer’s protocol. PvuII-HF and PstI-HF are high fidelity restriction enzymes, which dramatically reduce unspecific cuts.
FastDigest PvuII

Thermo Fisher Scientific

Protocol tips
Enzymes were used at a maximum concentration compatible with glycerol content lower than 4.75%. MvaI, HindIII, PvuII (Fastdigest™ series) and BcnI enzymes were from Thermo Scientific™. AvaII, HinP1I and EcoRV were from New England Biolabs.
PvuII NEB#R0151

New England BioLabs

Protocol tips
First, the Tet gene of pBR322 (Invitrogen) was removed by HindIII/PvuII (NEB) double digestion, followed by insertion of the linker, 5′-AGCTTAGATCTTGATCAGGATCCCAG-3′, which contains BglII and BamHI sites, to create pBR-Linker.
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